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| General Information | |||
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| Term | distal myopathy | ID (Ontology) | DOID:11720 (Human Disease) |
| Definition | A muscular dystrophy that is characterized by predominant weakness and atrophy beginning in the feet and/or hands. | ||
| Also Known As | "distal muscular dystrophy" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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myopathy |__muscular dystrophy |__distal myopathy 24 rec. |__distal myopathy 1 2 rec. |__distal myopathy 3 4 rec. |__distal myopathy 4 5 rec. |__distal myopathy Tateyama type |__distal myopathy with anterior tibial onset 1 rec. |__distal myopathy with rimmed vacuoles 1 rec. |__infantile-onset distal myopathy |__Miyoshi muscular dystrophy 3 rec. | |__Miyoshi muscular dystrophy 1 1 rec. | |__Miyoshi muscular dystrophy 2 | |__Miyoshi muscular dystrophy 3 2 rec. |__tibial muscular dystrophy 3 rec. |
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| Is a | muscular dystrophy | ||
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External Crossreferences & Linkouts
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ICD10CM:G71.09 MESH:D049310 MIM:PS160500 NCI:C84675 ORDO:399096 ORDO:5448 ORDO:59135 SNOMEDCT_US_2023_03_01:58795000 UMLS_CUI:C0751336 |
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